Father - Child Relations — The Dedicated African American Dad Study
Citation(s)
Julion W, Gross D, Barclay-McLaughlin G, Fogg L "It's not just about MOMMAS": African-American non-resident fathers' views of paternal involvement. Res Nurs Health. 2007 Dec;30(6):595-610. doi: 10.1002/nur.20223.
Julion W, Sumo J, Schoeny ME, Breitenstein SM, Bounds DT Recruitment, Retention, and Intervention Outcomes from the Dedicated African American Dad (DAAD) Study. J Urban Health. 2021 Oct;98(Suppl 2):133-148. doi: 10.1007/s11524-021-00549-8. Epub 2021 Jul
Julion WA, Breitenstein SM, Waddell D Fatherhood intervention development in collaboration with African American non-resident fathers. Res Nurs Health. 2012 Oct;35(5):490-506. doi: 10.1002/nur.21492. Epub 2012 Jun 8.
Julion WA, Sumo J, Bounds DT A tripartite model for recruiting African-Americans into fatherhood intervention research. Public Health Nurs. 2018 Sep;35(5):420-426. doi: 10.1111/phn.12411. Epub 2018 May 9.
African American Non-Resident Fatherhood Program: Effects on Child/Family Outcomes
Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.
Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.
Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.
Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.
Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.
